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| Formula | C28H35FO7 |
| Net Charge | 0 |
| Average Mass | 502.579 |
| Monoisotopic Mass | 502.23668 |
| SMILES | [H][C@@]12C[C@H]3OC4(CCCC4)O[C@@]3(C(=O)COC(C)=O)[C@@]1(C)C[C@H](O)[C@@]1(F)[C@@]2([H])CCC2=CC(=O)C=C[C@@]21C |
| InChI | InChI=1S/C28H35FO7/c1-16(30)34-15-22(33)28-23(35-26(36-28)9-4-5-10-26)13-20-19-7-6-17-12-18(31)8-11-24(17,2)27(19,29)21(32)14-25(20,28)3/h8,11-12,19-21,23,32H,4-7,9-10,13-15H2,1-3H3/t19-,20-,21-,23+,24-,25-,27-,28+/m0/s1 |
| InChIKey | ILKJAFIWWBXGDU-MOGDOJJUSA-N |
| Wikipedia |
|---|
| Roles Classification |
|---|
| Application: | anti-inflammatory drug A substance that reduces or suppresses inflammation. |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| amcinonide (CHEBI:31199) has parent hydride pregnane (CHEBI:8386) |
| amcinonide (CHEBI:31199) has role anti-inflammatory drug (CHEBI:35472) |
| amcinonide (CHEBI:31199) is a 11β-hydroxy steroid (CHEBI:35346) |
| amcinonide (CHEBI:31199) is a 20-oxo steroid (CHEBI:36885) |
| amcinonide (CHEBI:31199) is a 3-oxo-Δ1,Δ4-steroid (CHEBI:77166) |
| amcinonide (CHEBI:31199) is a acetate ester (CHEBI:47622) |
| amcinonide (CHEBI:31199) is a corticosteroid (CHEBI:50858) |
| amcinonide (CHEBI:31199) is a fluorinated steroid (CHEBI:50830) |
| amcinonide (CHEBI:31199) is a spiroketal (CHEBI:72600) |
| IUPAC Name |
|---|
| 16α,17α-(cyclopentane-1,1-diyldioxy)-9-fluoro-11β-hydroxy-3,20-dioxopregna-1,4-dien-21-yl acetate |
| INNs | Source |
|---|---|
| amcinonide | ChEBI |
| amcinónida | ChEBI |
| amcinonidum | ChEBI |
| Synonym | Source |
|---|---|
| Triamcinolonacetatcyclopentanonid | ChemIDplus |
| Manual Xrefs | Databases |
|---|---|
| D01387 | KEGG DRUG |
| DE2437847 | Patent |
| DB00288 | DrugBank |
| Amcinonide | Wikipedia |
| 150 | DrugCentral |
| Registry Numbers | Sources |
|---|---|
| CAS:51022-69-6 | ChemIDplus |